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Dose-dependent biological toxicity of green synthesized silver nanoparticles in rat’s brain

Metal nanoparticles, in general, and silver nanoparticles (AgNPs), in particular, have been the focus of numerous studies over the last two decades. Recently, the green synthesis of metal nanoparticles has been favored over chemical synthesis due to its low toxicity and easy preparation. The present...

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Autores principales: Tareq, Mai, Khadrawy, Yasser A., Rageh, Monira M., Mohammed, Haitham S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805464/
https://www.ncbi.nlm.nih.gov/pubmed/36587179
http://dx.doi.org/10.1038/s41598-022-27171-1
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author Tareq, Mai
Khadrawy, Yasser A.
Rageh, Monira M.
Mohammed, Haitham S.
author_facet Tareq, Mai
Khadrawy, Yasser A.
Rageh, Monira M.
Mohammed, Haitham S.
author_sort Tareq, Mai
collection PubMed
description Metal nanoparticles, in general, and silver nanoparticles (AgNPs), in particular, have been the focus of numerous studies over the last two decades. Recently, the green synthesis of metal nanoparticles has been favored over chemical synthesis due to its low toxicity and easy preparation. The present study aims to investigate the dose-dependent toxicity of green synthesized AgNPs on rats’ brains. Thirty-four Wistar male rats were divided into four groups. The first, second, and third groups were administered for 14 days with three different doses (0.5, 5, and 10 mg/kg) of AgNPs, respectively. The fourth group, which served as a control group, was given normal saline for the same period. The toxicity of the green synthesized AgNPs on the cortical and hippocampal levels of the oxidative stress markers (MDA, NO, and GSH) as well as the activity of acetylcholinesterase (AchE) and the monoamine neurotransmitters (DA, NE, and 5H-T) were investigated. AgNPs showed minimal oxidative stress in the cortex and hippocampus for the administered doses. However, AgNPs showed an inhibitory effect on AchE activity in a dose-dependent manner and a decrease in the 5H-T and NE levels. The green synthesized AgNPs showed an ultrastructural change in the cellular membranes of the neurons. The green synthesis of AgNPs has reduced their cytotoxic oxidative effects due to their capping with biologically compatible and boosting molecules such as flavonoids. However, another neurotoxicity was observed in a dose-dependent manner.
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spelling pubmed-98054642023-01-02 Dose-dependent biological toxicity of green synthesized silver nanoparticles in rat’s brain Tareq, Mai Khadrawy, Yasser A. Rageh, Monira M. Mohammed, Haitham S. Sci Rep Article Metal nanoparticles, in general, and silver nanoparticles (AgNPs), in particular, have been the focus of numerous studies over the last two decades. Recently, the green synthesis of metal nanoparticles has been favored over chemical synthesis due to its low toxicity and easy preparation. The present study aims to investigate the dose-dependent toxicity of green synthesized AgNPs on rats’ brains. Thirty-four Wistar male rats were divided into four groups. The first, second, and third groups were administered for 14 days with three different doses (0.5, 5, and 10 mg/kg) of AgNPs, respectively. The fourth group, which served as a control group, was given normal saline for the same period. The toxicity of the green synthesized AgNPs on the cortical and hippocampal levels of the oxidative stress markers (MDA, NO, and GSH) as well as the activity of acetylcholinesterase (AchE) and the monoamine neurotransmitters (DA, NE, and 5H-T) were investigated. AgNPs showed minimal oxidative stress in the cortex and hippocampus for the administered doses. However, AgNPs showed an inhibitory effect on AchE activity in a dose-dependent manner and a decrease in the 5H-T and NE levels. The green synthesized AgNPs showed an ultrastructural change in the cellular membranes of the neurons. The green synthesis of AgNPs has reduced their cytotoxic oxidative effects due to their capping with biologically compatible and boosting molecules such as flavonoids. However, another neurotoxicity was observed in a dose-dependent manner. Nature Publishing Group UK 2022-12-31 /pmc/articles/PMC9805464/ /pubmed/36587179 http://dx.doi.org/10.1038/s41598-022-27171-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tareq, Mai
Khadrawy, Yasser A.
Rageh, Monira M.
Mohammed, Haitham S.
Dose-dependent biological toxicity of green synthesized silver nanoparticles in rat’s brain
title Dose-dependent biological toxicity of green synthesized silver nanoparticles in rat’s brain
title_full Dose-dependent biological toxicity of green synthesized silver nanoparticles in rat’s brain
title_fullStr Dose-dependent biological toxicity of green synthesized silver nanoparticles in rat’s brain
title_full_unstemmed Dose-dependent biological toxicity of green synthesized silver nanoparticles in rat’s brain
title_short Dose-dependent biological toxicity of green synthesized silver nanoparticles in rat’s brain
title_sort dose-dependent biological toxicity of green synthesized silver nanoparticles in rat’s brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805464/
https://www.ncbi.nlm.nih.gov/pubmed/36587179
http://dx.doi.org/10.1038/s41598-022-27171-1
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